Phenylketonuria (PKU)

Question

08 Oct 2024

Answer :

Word Count : 229

Phenylketonuria (PKU) is a genetic disorder caused by a deficiency of the enzyme phenylalanine hydroxylase, which is crucial for metabolizing the amino acid phenylalanine into tyrosine. This autosomal recessive condition leads to the accumulation of phenylalanine in the blood, resulting in toxic effects on the brain if untreated. PKU is usually detected through newborn screening programs, where _________ ______ _____ __________ ____ __________.
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